This is a prospective investigation which aims to address key challenges to the design of clinical trials to prevent the onset of Huntington's disease (HD). The project will provide necessary psychometric data for clinical outcome assessments (COAs) and biomarkers (BMs) in the cerebral spinal fluid (CSF) to address questions of central importance to the success of these measures for premanifest clinical trials. Of the 258 participants: 52 will be low risk of motor diagnosis, 102 high risk of motor diagnosis, 52 with diagnosed HD (stages I or II), and 52 healthy controls. Participants can expect to be in the study for up to 2 years.
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Unified Huntington's Disease Rating Scale (UHDRS) Diagnostic Confidence Level
Timeframe: baseline
Unified Huntington's Disease Rating Scale (UHDRS) Diagnostic Confidence Level
Timeframe: 1 years
Unified Huntington's Disease Rating Scale (UHDRS) Diagnostic Confidence Level
Timeframe: 2 years
Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score
Timeframe: baseline
Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score
Timeframe: 1 year
Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score
Timeframe: 2 years
Unified Huntington's Disease Rating Scale (UHDRS) Total Functional Capacity
Timeframe: baseline
Unified Huntington's Disease Rating Scale (UHDRS) Total Functional Capacity
Timeframe: 1 year
Unified Huntington's Disease Rating Scale (UHDRS) Total Functional Capacity
Timeframe: 2 years